Importing FDA-Regulated Products: The Import Process (Mandarin Version) - 进口FDA监管产品:进口流程

U.S. Food and Drug Administration
U.S. Food and Drug Administration
990 بار بازدید - پارسال - FDA所监管产品的进口流程主要分为以下五个阶段:第一阶段:进口准备;第二阶段:报关单提交;第三阶段:报关单审核;第四阶段:检查和抽样;第五阶段:合规审查。在进口流程的任何环节,如果FDA认为您的产品无需进一步审核或检查,您的产品将被放行。否则,FDA将继续对产品进行审查直至可以做出最终的准许入境决定。以下是这五个进口阶段的详细说明。There are five major phases
FDA所监管产品的进口流程主要分为以下五个阶段:第一阶段:进口准备;第二阶段:报关单提交;第三阶段:报关单审核;第四阶段:检查和抽样;第五阶段:合规审查。在进口流程的任何环节,如果FDA认为您的产品无需进一步审核或检查,您的产品将被放行。否则,FDA将继续对产品进行审查直至可以做出最终的准许入境决定。以下是这五个进口阶段的详细说明。

There are five major phases to the FDA’s import process: One - Preparing to import. Two - Entry submission. Three - Entry review. Four - Examination and sampling. And five - Compliance review. If, at any point during the import process, the FDA determines that your products do not need further review or examination, they’ll be released. Otherwise, the agency will continue to review until a final admissibility decision can be made. Let’s look at these five import phases in more detail.
پارسال در تاریخ 1401/12/11 منتشر شده است.
990 بـار بازدید شده
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